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34
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T2253 |
TCS PIM-1 1
3-氰基-4-苯基-6-(3-溴-6-羟基苯基)-2(1H)-吡啶酮,SC 204330 |
Pim | Chromatin/Epigenetic; JAK/STAT signaling |
TCS PIM-1 1 (SC 204330) 是一种特异性有效的 ATP 竞争性 Pim-1 激酶抑制剂,IC50为 50 nM,对 MEK1/MEK2 和 Pim-2 表现出良好的特异性,IC50值大于 20000 nM。 | |||
T4215 |
TCS-PIM-1-4a
5-[[3-(三氟甲基)苯基]亚甲基]-2,4-噻唑烷二酮,SMI-4a |
Apoptosis; Pim | Apoptosis; Chromatin/Epigenetic; JAK/STAT signaling |
TCS-PIM-1-4a (SMI-4a) 是一种泛-Pim 激酶抑制剂,可通过激活 AMPK 来阻断 mTORC1的活性。它可杀死多种髓样和淋巴样细胞系,IC50值为 0.8 μM 至 40 μM。 | |||
T9229 |
Pim-1/2 kinase inhibitor 1
|
Pim | Chromatin/Epigenetic; JAK/STAT signaling |
Pim-1/2 kinase inhibitor 1 是一种具有口服活性的 Pim-1/2 激酶抑制剂。Pim-1/2 kinase inhibitor 1 能阻断 Pim 激酶磷酸化肽的能力,并且抑制4E-BP1和p27Kip1的Pim 蛋白激酶定向磷酸化。Pim-1/2 kinase inhibitor 1 可用于癌症,尤其是前列腺癌的研究。 | |||
T3058 |
(Z)-SMI-4a
TCS PIM-1 4a,SMI-4a |
Pim | Chromatin/Epigenetic; JAK/STAT signaling |
(Z)-SMI-4a (TCS PIM-1 4a) 是一种选择性的,细胞可渗透的且具有 ATP 竞争性的 Pim-1抑制剂,IC50为 24 μM,Ki 为 0.6 μM。它还抑制 Pim-2,IC50为 100 μM,具有抗癌活性。 | |||
T6148 |
CX-6258 hydrochloride
CX-6258 HCl,Pim-Kinase Inhibitor X |
Pim | Chromatin/Epigenetic; JAK/STAT signaling |
CX-6258 hydrochloride (Pim-Kinase Inhibitor X) 是一种强效选择性的泛 Pim 激酶抑制剂,对Pim-1、Pim-2 和 Pim-3 作用的IC50值分别为 5、25 和 16 nM。 | |||
T3078 |
SGI-1776
SGI-1776 free base,Pim-Kinase Inhibitor IX |
Apoptosis; FLT; Pim; Autophagy | Angiogenesis; Apoptosis; Autophagy; Chromatin/Epigenetic; JAK/STAT signaling; Tyrosine Kinase/Adaptors |
SGI-1776 (Pim-Kinase Inhibitor IX) 是一种Pim 抑制剂,抑制 Pim-1、Pim-2 和 Pim-3 的活性,IC50值分别为 7 nM、363 nM 和 69 nM。 | |||
T83627 |
Pim-1 kinase inhibitor 8
|
Pim; PKC | Chromatin/Epigenetic; Cytoskeletal Signaling; JAK/STAT signaling |
Pim-1 kinase inhibitor 8 是一种高效的 Pim-1 kinase 抑制剂,具有抗癌活性,可有效抑制细胞迁移。Pim-1 kinase inhibitor 8 对 MCF-7 和 HepG2 细胞有细胞毒性,是研究乳腺癌的候选化合物。 | |||
T40319 |
PIM-IN-1
|
||
PIM-IN-1 is a pan-PIM kinase inhibitor (KG-1, EC 50 = 61 nM; pS6, EC 50 = 71 nM). | |||
T77526 |
Pim-1 kinase inhibitor 4
|
Apoptosis; Pim | Apoptosis; Chromatin/Epigenetic; JAK/STAT signaling |
Pim-1 kinase inhibitor 4 是一种高效的 Pim-1 激酶 抑制剂,IC50 值为 17.01 nM。Pim-1 kinase inhibitor 4 还具有抗氧化活性和潜在的抗癌活性,对 DPPH 有抑制作用。Pim-1 kinase inhibitor 4 促进 PC-3 细胞凋亡 (apoptosis),对 PC-3 细胞生长有抑制作用,IC50 为 16 nM。Pim-1 kinase inhibitor 4 可用于研究前列腺癌。 | |||
T5093 |
Pim1/AKK1-IN-1
LKB1/AAK1 dual inhibitor,MDK-2275 |
Pim; Hippo pathway | Chromatin/Epigenetic; JAK/STAT signaling; Stem Cells |
Pim1/AKK1-IN-1 (LKB1/AAK1 dual inhibitor) 是多种酶抑制剂,能够作用于Pim1、AKK1、MST2 和 LKB1,Kd 值分别为 35、53、75 和 380 nM,还抑制 MPSK1 和 TNIK。 | |||
T40092 |
MNK/PIM-IN-1
|
||
MNK/PIM-IN-1 is a novel dual inhibitor targeting both MNK and PIM pathways, characterized by its favorable pharmacokinetic profile. | |||
T12473 |
PIM-447 dihydrochloride
LGH447 dihydrochloride |
Others | Others |
PIM-447 dihydrochloride is an orally available and selective inhibitor of pan-PIM kinase(Ki values of 6, 18, and 9 pM for PIM1, PIM2, and PIM3, respectively). | |||
T23158 |
PIM-1 Inhibitor 2
|
Others | Others |
PIM-1 Inhibitor 2 is an effective Pim-1 kinase inhibitor (Ki = 91 nM). | |||
T2300 |
AZD1208
|
Apoptosis; Pim; Autophagy | Apoptosis; Autophagy; Chromatin/Epigenetic; JAK/STAT signaling |
AZD1208 是一种具有口服活性的高度选择性PIM 抑制剂。 | |||
T4523 |
TP-3654
|
Pim | Chromatin/Epigenetic; JAK/STAT signaling |
TP3654是一种Pim 激酶抑制剂,对Pim-1和Pim-3的Ki 值分别为5和42 nM。 | |||
T1834 |
CX-6258
CX 6258 |
Pim | Chromatin/Epigenetic; JAK/STAT signaling |
CX-6258是一种强效选择性的泛 Pim 激酶抑制剂,对Pim-1、Pim-2 和 Pim-3 作用的IC50值分别为 5、25 和 16 nM。 | |||
T71558 | Pim-IN-14j | ||
Pim-IN-14j is a potent, highly selective, and orally bioavailable inhibitor of PIM-1 kinases. | |||
T81460 |
PIM-IN-2
|
Pim | Chromatin/Epigenetic; JAK/STAT signaling |
PIM-IN-2是Pim激酶抑制剂,具有25 nM 的半抑制浓度(IC50)。它能增强细胞存活、防止凋亡,并在多种人类肿瘤中高表达。 | |||
T3989 |
SMI-16a
PIM1/2 Kinase Inhibitor VI |
Pim | Chromatin/Epigenetic; JAK/STAT signaling |
SMI-16a (PIM1/2 Kinase Inhibitor VI) 是选择性 Pim 激酶抑制剂,对 Pim1、Pim2 和 PC3 细胞的 IC50值分别为0.15、0.02 和48 μM。 | |||
T60972 | Pim-1 kinase inhibitor 1 | ||
Pim-1 kinase inhibitor 1 可用于癌症领域研究, 通过促进细胞凋亡对多种癌细胞系表现出抗癌活性。Pim-1 kinase inhibitor 1 是一种Pim-1 激酶抑制剂 (IC50 = 0.11 μM)。 | |||
T78980 |
Pim-1 kinase inhibitor 5
|
Pim | Chromatin/Epigenetic; JAK/STAT signaling |
Pim-1 kinase inhibitor 5 (Compound 4c)是一种选择性Pim-1激酶抑制剂,具有0.61 μM的半抑制浓度(IC50)。该化合物对HepG2、MCF-7、PC3和HCT-116癌细胞系表现出细胞毒性,其IC50s值介于6.95至20.19 μM之间。 | |||
T61510 | PIM-1/HDAC-IN-1 | ||
PIM-1/HDAC-IN-1 (compound 4d) is a potent inhibitor of PIM-1, with an IC 50 of 343.87 nM. It also exhibits strong inhibitory activity and selectivity against HDAC 1 and HDAC 6, with IC 50 values of 63.65 and 62.39 nM, respectively. Furthermore, PIM-1/HDAC-IN-1 demonstrates apoptosis-inducing potential in MCF-7 cell lines, specifically inducing pre-G1 apoptosis and causing cell cycle arrest at the G2/M phase [1]. | |||
T12477 |
Uzansertib phosphate
INCB053914 phosphate |
Pim | Chromatin/Epigenetic; JAK/STAT signaling |
Uzansertib phosphate (INCB053914 phosphate) 是一种可口服的 ATP 竞争性泛-PIM 激酶抑制剂,对多种血液肿瘤细胞系具有广泛的抗增殖活性,对 PIM1、PIM2 和 PIM3 的 IC50分别为 0.24 、30 和 0.12 nM。 | |||
T61074 | Pim-1 kinase inhibitor 3 | ||
Pim-1 kinase inhibitor 3 (Compound H5) 是一种有效的Pim-1激酶抑制剂,IC50为 35.13 nM。 | |||
T62001 | Pim-1 kinase inhibitor 2 | ||
Pim-1 kinase inhibitor 2 (Compound 13) 为高效Pim-1激酶抑制剂,能诱导细胞凋亡(apoptosis),显示出在癌症疾病研究中的应用潜力。 | |||
T12475 |
PIM447
LGH447 |
Others | Others |
PIM447 is a potent, orally available, and selective inhibitor of pan-PIM kinase(PIM1, PIM2, and PIM3 with Ki values of 6, 18, and 9 pM , respectively). | |||
T13425 |
(1S,3R,5R)-PIM447 dihydrochloride
(1S,3R,5R)-LGH447 dihydrochloride |
CDK | Cell Cycle/Checkpoint |
(1S,3R,5R)-PIM447 (dihydrochloride) an inhibitor of PIM(IC50 of 0.095 μM for Pim1, 0.522 μM for Pim2 and 0.369 μM for Pim3). | |||
T15376 | GDC-0339 | Pim | Chromatin/Epigenetic; JAK/STAT signaling |
GDC-0339 是可口服的、耐受性良好的泛 Pim 激酶高效抑制剂,具有研究多发性骨髓瘤的潜力,对 Pim1、Pim2 和 Pim3 作用的 Ki 值分别为 0.03、0.1 和 0.02 nM。 | |||
T24166 |
Inecalcitol
TX 522,TX-522,TX522,伊奈骨化醇 |
Apoptosis | Apoptosis |
Inecalcitol (TX 522) 是一种独特的维生素 D3 类似物,可诱导细胞凋亡,有抗癌活性。它是一种具有口服活性维生素 D 受体激动剂,Kd 为 0.53 nM。 | |||
T12474 |
PIM1-IN-1
|
Pim | Chromatin/Epigenetic; JAK/STAT signaling |
PIM1-IN-1 is a potent and highly selective inhibitor of PIM1/3(IC50s of 7, 5530 and 70 nM for PIM1, PIM2, and PIM3, respectively),with Antiproliferative and anti-cancer activity. | |||
T71556 |
MK-1496
|
||
MK1496 is a n orally bioavailable Polo-like kinase 1 (Plk1) inhibitor with potential antineoplastic activity. Polo-like kinase 1 inhibitor MK1496 selectively inhibits Plk1, inducing selective G2/M arrest followed by apoptosis in a variety of tumor cells while causing reversible cell arrest at the G1 and G2 stage without apoptosis in normal cells. Plk1, named after the polo gene of Drosophila melanogaster, is a serine/threonine protein kinase involved in regulating mitotic spindle function in a n... | |||
T63720 | PIM1-IN-3 | ||
PIM1-IN-3 (Compound HL8) 是一种 PIM1 的有效抑制剂,能够选择性抑制 PIM-1 酶,可有效的诱导 Colo320 细胞凋亡。PIM1-IN-3 对癌症疾病表现出研究潜力。 | |||
T62188 |
PIM1-IN-6
|
||
PIM1-IN-6 (compound 5h) 是一种 PIM-1 的有效抑制剂 (IC50: 0.60 μM)。PIM1-IN-6 对 HCT-116 和 MCF-7 细胞具有较高的细胞毒作用,他们的 IC50 值分别为 1.51 和 15.2 μM。 | |||
T61700 | PIM1-IN-7 | ||
PIM1-IN-7 (compound 6c) is a powerful inhibitor of PIM-1, effectively suppressing its activity with an IC50 of 0.67 μM. This compound also exhibits significant cytotoxicity against HCT-116 and MCF-7 cells, as demonstrated by their respective IC50 values of 42.9 and 7.68 μM [1]. | |||
T73247 | PIM1-IN-4 | Pim | Chromatin/Epigenetic; JAK/STAT signaling |
PIM1-IN-4(Compound 8)为PIM1高效抑制剂,对SGK-1、PKA、CaMK-1、GSK3β及MSK1五种酶亦展现出显著抑制效应,表现出其在癌症疾病研究中的应用潜力。 | |||
T63071 |
CDK6/PIM1-IN-1
|
||
CDK6/PIM1-IN-1 是一种平衡的、有效的、双重 CDK6 (IC50: 39 nM) 和 PIM1 (IC50: 88 nM) 抑制剂。CDK6/PIM1-IN-1 对 CDK4 表现出抑制作用,其 IC50 值为 3.6 nM。CDK6/PIM1-IN-1 能够明显抑制急性髓系白血病 (AML) 细胞增殖,将细胞周期阻滞在 G1 期并诱导细胞凋亡。CDK6/PIM1-IN-1 表现出抗 AML 活性。 | |||
T63550 | (1S,3R,5R)-PIM447 dihydrochloride | ||
(1S,3R,5R)-PIM447 (dihydrochloride) 是一种 PIM 的抑制剂,能够Pim1 (IC50: 0.095 μM)、Pim2 (IC50: 0.522 μM) 和 Pim3 (IC50: 0.369 μM)。 | |||
T16994 |
Pimitespib
TAS-116 |
HSP | Cytoskeletal Signaling; Metabolism |
Pimitespib (TAS-116) 是一种 ATP 竞争性和高度特异性的 HSP90α/HSP90β 抑制剂,Ki 值分别为 34.7 nM 和 21.3 nM。 | |||
T25263 |
Clopimozide
R-29764,NSC-335305,NSC 335305,NSC335305,R 29764 |
Calcium Channel | Membrane transporter/Ion channel; Metabolism |
Clopimozide (R-29764) 可作为一种钙通道拮抗剂,抑制 [3H] 尼群地平结合。Clopimozide 是一种新型且可口服的长效抗精神分裂症精神安定化合物。 | |||
T12489 |
Pimethixene
Calmixen,匹美噻吨,Pimetixene |
Dopamine Receptor; 5-HT Receptor; AChR; Histamine Receptor | GPCR/G Protein; Immunology/Inflammation; Neuroscience |
Pimethixene (Calmixen) 是抗组胺和抗血清素剂,用作抗偏头疼剂。它是高效多靶点拮抗剂。 | |||
T8920 |
Sepimostat
|
iGluR | Membrane transporter/Ion channel; Neuroscience |
Sepimostat 通过 NR2B 亚基的 Ifenprodil 结合位点的 NR2B N-甲基-D-天冬氨酸受体拮抗作用表现出神经保护活性。它抑制 Ifenprodil 结合的 Ki 值为27.7 µM。 | |||
T16536 |
Pimonidazole hydrochloride
|
||
Pimonidazole hydrochloride 通过与大分子共价结合或在其硝基还原后形成还原性代谢物在缺氧细胞中积累。 可用于肿瘤缺氧的定性和定量评估。 它是一种新型的缺氧标志物,用于肿瘤缺氧和肿瘤细胞增殖的互补研究。 | |||
T6277 |
Doramapimod
BIRB 796,达马莫德,度马莫德 |
Raf; p38 MAPK; Autophagy | Autophagy; MAPK |
Doramapimod (BIRB 796) 是一种具有口服活性的p38 MAPK 抑制剂,Kd 值为0.1nM。它也抑制B-Raf 和 Abl,IC50分别为 83 nM 和 14.6 μM。 | |||
T6946 |
Pimavanserin tartrate
ACP-103,ACP-103 tartrate,Nuplazid,Pimavanserin,匹莫范色林 |
5-HT Receptor | GPCR/G Protein; Neuroscience |
Pimavanserin tartrate (Nuplazid) 是一种有效的5-HT 2A 受体反向激动剂,pIC50和 pKi 值分别为8.73和9.3,用于治疗与帕金森病相关的精神病。 | |||
T1162 |
Acipimox
Olbemox,K-9321,阿西莫司,阿昔莫司 |
Others | Others |
Acipimox (K-9321) 是烟酸类似物,能够急性抑制脂解作用,抑制全身游离脂肪水平,改善胰岛素敏感性。 | |||
T6297 |
Alvespimycin hydrochloride
BMS 826476,NSC 707545,阿螺旋霉素盐酸盐,KOS-1022,17-DMAG hydrochloride,Alvespimycin (17-DMAG) HCl |
Apoptosis; HSP | Apoptosis; Cytoskeletal Signaling; Metabolism |
Alvespimycin hydrochloride (BMS 826476) 是一种Hsp90抑制剂,结合到 Hsp90,EC50为 62±29 nM。 | |||
T37979 |
N-Desmethyl Pimavanserin
AC-279 |
5-HT Receptor | GPCR/G Protein; Neuroscience |
N-Desmethyl Pimavanserin (AC-279) 是 Pimavanserin (一种 5-HT2A 受体反向激动剂)的活性代谢物,可用于治疗失眠等睡眠障碍。 | |||
T0868 |
Cefepime Dihydrochloride Monohydrate
Cefepime HCl,头孢吡肟二盐酸盐一水合物 |
Antibacterial; Antibiotic; Antifection | Microbiology/Virology |
Cefepime Dihydrochloride Monohydrate (Cefepime HCl) 是一种广谱头孢菌素,对革兰氏阳性菌和革兰氏阴性菌有更高的覆盖率。 | |||
T2648 |
Pimecrolimus
SDZ-ASM 981,ASM 981,吡美莫司 |
Others | Others |
Pimecrolimus (SDZ-ASM 981) 是一种免疫亲和素配体,能与胞质受体特异性的结合。 | |||
T18363 |
Monoethyl pimelate
|
Others; PROTAC Linker | Others; PROTAC |
Monoethyl pimelate 是一种属于 alkyl/ether 类的 PROTAC linker 可用于特异性的 BCL-XLPROTAC 降解剂 (S,R,S)-AHPC-Me-C7 ester 的合成。 |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
TQ0201 |
Hispidulin
Dinatin |
Pim | Chromatin/Epigenetic; JAK/STAT signaling |
Hispidulin 是存在于豚草中的一种黄酮,是Pim-1抑制剂,IC50值为2.71 μM。 | |||
T8114 |
Quercetagetin
栎草亭,6-Hydroxyquercetin |
Pim | Chromatin/Epigenetic; JAK/STAT signaling |
Quercetagetin (6-Hydroxyquercetin) 是存在于万寿菊中的一种类黄酮,是一种选择性和细胞渗透性的pim-1激酶抑制,IC50为 0.34 μM,具有抗炎和抗肿瘤活性。 | |||
T6290 |
Tanespimycin
坦螺旋霉素,17-AAG,CP 127374,NSC 330507,KOS 953 |
Apoptosis; Mitophagy; HSP; Antibacterial; Antibiotic; Autophagy | Apoptosis; Autophagy; Cytoskeletal Signaling; Metabolism; Microbiology/Virology |
Tanespimycin (KOS 953) 是一种 Hsp90 抑制剂,可选择性抑制 BT474 肿瘤细胞 Hsp90,IC50为 5 nM。它消耗细胞内 STK38/NDR1,并降低 STK38 激酶活性,还能下调stk38基因表达。 | |||
T3906 |
Epimedin A
|
Others | Others |
Epimedin A 是一种提取自草本淫羊藿中的天然化合物。 | |||
TN1610 |
Epimagnolin A
|
Parasite | Microbiology/Virology |
Epimagnolin A 是一种糠醛木脂素,具有中等的抗疟原虫活性,IC50值为5.7 μg/mL。 | |||
T6S2146 |
Epimedin B
朝藿定B,Epmedin B |
Others | Others |
Epimedin B (Epmedin B) 是一种天然活性成分,来自淫羊藿,据报道其就有抗骨质疏松症的潜能。 | |||
T4593 |
ISOPIMPINELLIN
5,8-Dimethoxypsoralen,异茴芹内酯,4,9-Dimethoxypsoralen |
Antiviral; DNA/RNA Synthesis; Parasite | Cell Cycle/Checkpoint; DNA Damage/DNA Repair; Immunology/Inflammation; Microbiology/Virology |
Isopimpinellin (4,9-Dimethoxypsoralen) 是从 Pimpinella saxifrage 根部分离得到的一种天然产物,具有抗病毒和抗利什曼病活性。 | |||
T5S2139 |
Epimedin A1
朝藿定A1,Hexandraside F |
Others | Others |
Epimedin A1 (Hexandraside F) 是一种黄酮类化合物,从常用中药淫羊藿中提取得到。 | |||
T4795 |
Pimelic acid
Pileric acid,1,7-Heptanedioic acid,庚二酸,1,5-Pentanedicarboxylic acid |
Others; Endogenous Metabolite | Metabolism; Others |
Pimelic acid (1,5-Pentanedicarboxylic acid) 的衍生物能够参与赖氨酸的生物合成。 | |||
TN3972 |
Epimedokoreanin B
|
Apoptosis; Others; Antibacterial | Apoptosis; Microbiology/Virology; Others |
Epimedokoreanin B (EKB) 是一种从韩国淫羊藿中分离出的异戊烯化类黄酮,在人非小细胞肺癌(NSCLC)A549和NCI-H292细胞中展现出抗癌活性。Epimedokoreanin B 还具有抗炎和抗菌活性,可有清除 DPPH 自由基的活性,能以剂量依赖的方式抑制 MCF-7 和 HepG2 的增殖。Epimedokoreanin B 能显著抑制 N (δ) -(羧甲基)赖氨酸(CML)和 N (Ï) -(羧甲基)精氨酸(CMA)的形成,可通过抑制高级糖化终产物(AGEs)预防糖尿病的临床并发症。 | |||
TN1611 |
Epimedoside A
淫羊藿苷 A,淫羊藿新苷A |
Others | Others |
Epimedoside A 是一种黄酮类化合物,从Epimedium wushanense 根中分离得到,在体外具有显著的抗氧化活性。 | |||
T5776 |
pimpinellin
|
Apoptosis; Anti-infection | Apoptosis; Microbiology/Virology |
Pimpinellin 是贯众的一种成分,可通过诱导肿瘤细胞凋亡抑制肿瘤细胞的生长,可作为具有 GABA 受体活性的蛋白质的拮抗剂。 | |||
TN2639 | 15-Isopimarene-8,18-diol | Others | Others |
15-Isopimarene-8,18-diol 是一种天然产物,可用于生命科学领域的相关研究。其产品编号为 TN2639,CAS号为 73002-86-5。 | |||
TN5663 | Epimedonin J | ||
Epimedonin J 是一种天然产物,可用于生命科学领域的相关研究。其产品编号为 TN5663,CAS号为 2222285-84-7。 | |||
TN2611 |
13-Epimanool
|
Others | Others |
13-Epimanool是一种天然产物,属于唇形科鼠尾草属,其产品编号为 TN2611,CAS号为 1438-62-6。13-Epimanool可用作对照参考。 | |||
TN1835 |
Epimedoside
Korepimedoside A,朝鲜淫羊藿苷A |
Others | Others |
Korepimedoside A is a natural product from Epimedium koreanum. | |||
TN6294 | 2α-Acetoxy-14,15-cyclopimara-7β,16-diol | ||
2α-Acetoxy-14,15-cyclopimara-7β,16-diol 是一种天然产物,可用于生命科学领域的相关研究。其产品编号为 TN6294,CAS号为 2011034-27-6。 | |||
TN5662 | Epimedonin I | ||
Epimedonin I 是一种天然产物,可用于生命科学领域的相关研究。其产品编号为 TN5662,CAS号为 2222285-83-6。 | |||
TN5659 |
7-O-Methylepimedonin G
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7-O-Methylepimedonin G 是一种天然产物,可用于生命科学领域的相关研究。其产品编号为 TN5659,CAS号为 2220243-40-1。 | |||
TN3971 |
Epimedin K
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Others | Others |
Epimedin K is a natural product from Epimedium koreanum NAKAI (Berberidaceae). | |||
TN3260 |
8(14),15-Isopimaradien-3-ol
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Calcium Channel; Antifection | Membrane transporter/Ion channel; Metabolism; Microbiology/Virology |
ent-8(14),15-pimaradien-3beta-ol (8(14),15-Isopimaradien-3-ol) can induce vascular relaxation. It displays high antibacterial activities (MIC values lower than 10 microg /mL for most pathogens). | |||
TN3970 |
Epimedin B1
朝藿定B1 |
Others | Others |
Epimedin B1 是一种天然产物,可用于生命科学领域的相关研究。其产品编号为 TN3970,CAS号为 133137-58-3。 | |||
TN5953 | 3-Epimeliasenin B | ||
3-Epimeliasenin B 是一种天然产物,可用于生命科学领域的相关研究。其产品编号为 TN5953,CAS号为 1222475-77-5。 | |||
TN5664 |
Epimedonin K
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Epimedonin K 是一种天然产物,可用于生命科学领域的相关研究。其产品编号为 TN5664,CAS号为 2222285-85-8。 | |||
TN2075 |
Pimaric acid
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MMP; p38 MAPK; NF-κB | MAPK; NF-κB; Proteases/Proteasome |
Pimaric acid has potent anti-atherosclerotic activity with inhibitory action on matrix metalloproteinase-9 production and cell migration in TNF-α±-induced human aortic smooth muscle cells. | |||
TN3935 | ent-14,16-Epoxy-8-pimarene-3,15-diol | Others | Others |
ent-14,16-Epoxy-8-pimarene-3,15-diol 是一种天然产物,可用于生命科学领域的相关研究。其产品编号为 TN3935,CAS号为 1188281-98-2。 | |||
T39445 |
Korepimedoside C
Epimedin I,朝藿苷丙 |
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Korepimedoside C, also known as Epimedin I, is a flavonol glycoside derived from the aerial parts of Epimedium koreanum Nakai. Epimedium koreanum Nakai is a renowned Chinese herbal medicine that has been extensively studied for its potential in addressing impotence, osteoporosis, immune suppression, and cardiovascular diseases. | |||
TN1009 |
Epimagnolin B
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NF-κB; NO Synthase; Prostaglandin Receptor | GPCR/G Protein; Immunology/Inflammation; NF-κB |
Epimagnolin B 是一种双环氧木质素,分离自木兰中。它能够抑制 LPS 激活的小胶质细胞中 NO 的产生。它具有抗过敏以及抗炎作用。 | |||
T82027 |
Isopimarol acetate
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Isopimarol acetate是Nepeta tuberosa subsp. reticulata中提取的一种天然产物。 | |||
TN3261 | 8(14),15-Isopimaradiene-3,18-diol | Others | Others |
8(14),15-Isopimaradiene-3,18-diol 是一种天然产物,可用于生命科学领域的相关研究。其产品编号为 TN3261,CAS号为 59219-64-6。 | |||
TN5667 | Epimedonin G | ||
Epimedonin G 是一种天然产物,可用于生命科学领域的相关研究。其产品编号为 TN5667,CAS号为 2222285-80-3。 | |||
TN5468 |
Epimedonin L
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Epimedonin L 是一种天然产物,可用于生命科学领域的相关研究。其产品编号为 TN5468,CAS号为 2215102-38-6。 | |||
TN4319 |
Isopimaric acid
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Antifection | Microbiology/Virology |
Isopimaric acid is active against MDR and MRSA strains of S. aureus which are becoming increasingly resistant to antibiotics, the minimum inhibitory concentrations (MIC) are 32-64 microg/mL . Isopimaric acid is also possible that an antagonistic interacti | |||
TN5668 |
Epimedonin H
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Epimedonin H 是一种天然产物,可用于生命科学领域的相关研究。其产品编号为 TN5668,CAS号为 2222285-82-5。 |